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Tip Implant universal curette Mini L ErgoMix

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 283MTIEMModel Tip for dental hand instrument, titanium curette for implant maintenance

by LM-Instruments Oy

Identity

Trade Name
Tip Implant universal curette Mini L ErgoMix EUDAMED
LMDental FDA UDI
Generic Name
Periodontal curette FDA UDI
Device Name
Periodontal hand instrument EUDAMED
Tip Implant universal curette Mini L ErgoMix, Periodontics FDA UDI
Model / Reference
283MTIEM EUDAMEDFDA UDI
Tip for dental hand instrument, titanium curette for implant maintenance EUDAMED
Description
Tip Implant universal curette Mini L ErgoMix, Periodontics FDA UDI

Identifiers

Primary DI / UDI-DI
06438311211541 EUDAMEDFDA UDI
Basic UDI-DI
6438311PERIO1r06S EUDAMED
B-06438311211541 EUDAMED
FDA Product Code
DZN FDA UDI
EMDN Code
L159001 DENTAL AND PERIODONTAL CURETTES, REUSABLE EUDAMED
GMDN Term
Periodontal curette FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.4565 FDA UDI
Market of Registration
Finland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Tip Implant universal curette Mini L ErgoMix by LM-Instruments Oy — Class I — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
LM-Instruments Oy
EUDAMED SRN
FI-MF-000006705

Sources (3)

  • EUDAMED c34fec95-b31c-4ba2-9286-89d105df1480 61 fields · synced Jun 18, 2026
  • EUDAMED 20c00807-bde3-4ecf-9021-8c09692190f3 61 fields · synced May 19, 2026
  • FDA UDI 1c9566a5-6b47-4b7c-a2b3-7d1c9268794a 33 fields · synced May 30, 2026